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Ganitumab and metformin plus standard neoadjuvant therapy in stage 2/3 breast cancer.

Authors :
Yee D
Isaacs C
Wolf DM
Yau C
Haluska P
Giridhar KV
Forero-Torres A
Jo Chien A
Wallace AM
Pusztai L
Albain KS
Ellis ED
Beckwith H
Haley BB
Elias AD
Boughey JC
Kemmer K
Yung RL
Pohlmann PR
Tripathy D
Clark AS
Han HS
Nanda R
Khan QJ
Edmiston KK
Petricoin EF
Stringer-Reasor E
Falkson CI
Majure M
Mukhtar RA
Helsten TL
Moulder SL
Robinson PA
Wulfkuhle JD
Brown-Swigart L
Buxton M
Clennell JL
Paoloni M
Sanil A
Berry S
Asare SM
Wilson A
Hirst GL
Singhrao R
Asare AL
Matthews JB
Hylton NM
DeMichele A
Melisko M
Perlmutter J
Rugo HS
Fraser Symmans W
Van't Veer LJ
Berry DA
Esserman LJ
Source :
NPJ breast cancer [NPJ Breast Cancer] 2021 Oct 05; Vol. 7 (1), pp. 131. Date of Electronic Publication: 2021 Oct 05.
Publication Year :
2021

Abstract

I-SPY2 is an adaptively randomized phase 2 clinical trial evaluating novel agents in combination with standard-of-care paclitaxel followed by doxorubicin and cyclophosphamide in the neoadjuvant treatment of breast cancer. Ganitumab is a monoclonal antibody designed to bind and inhibit function of the type I insulin-like growth factor receptor (IGF-1R). Ganitumab was tested in combination with metformin and paclitaxel (PGM) followed by AC compared to standard-of-care alone. While pathologic complete response (pCR) rates were numerically higher in the PGM treatment arm for hormone receptor-negative, HER2-negative breast cancer (32% versus 21%), this small increase did not meet I-SPY's prespecified threshold for graduation. PGM was associated with increased hyperglycemia and elevated hemoglobin A1c (HbA1c), despite the use of metformin in combination with ganitumab. We evaluated several putative predictive biomarkers of ganitumab response (e.g., IGF-1 ligand score, IGF-1R signature, IGFBP5 expression, baseline HbA1c). None were specific predictors of response to PGM, although several signatures were associated with pCR in both arms. Any further development of anti-IGF-1R therapy will require better control of anti-IGF-1R drug-induced hyperglycemia and the development of more predictive biomarkers.<br /> (© 2021. The Author(s).)

Details

Language :
English
ISSN :
2374-4677
Volume :
7
Issue :
1
Database :
MEDLINE
Journal :
NPJ breast cancer
Publication Type :
Academic Journal
Accession number :
34611148
Full Text :
https://doi.org/10.1038/s41523-021-00337-2